1. Volume 17, Issue 1, Pages 43-53 (July 1996)
Asymmetric Localization of a Mammalian Numb Homolog during Mouse Cortical Neurogenesis 
Weimin Zhong, John N Feder, Ming-Ming Jiang, Lily Yeh Jan, Yuh Nung Jan 
Neuron 
Volume 17, Issue 1, Pages (July 1996)
DOI: /S (00)

2. Figure 1 Sequence Analysis of Mouse numb
(A) Predicted amino acid sequence of m-numb. The first methionine is numbered 1. Underlined amino acids represent a presumptive PTB domain. The bracketed sequence represents a potential SH3 binding site.
(B) Sequence comparison between mouse and Drosophila Numb. Sequences were aligned using the GCG bestfit program. Vertical lines represent identical amino acids.
(C) Schematic diagrams of mouse and Drosophila Numb. Crosshatching indicates the conserved Numb domain, with 63.3% identity in amino acids.
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3. Figure 2 Mouse numb Expression in Adult and Embryonic Mice
(A) Northern blot analysis of m-numb expression in adult mouse organs; 5 μg of poly(A)+ RNA was used in each lane. A glyceraldehyde-3-phosphate dehydrogenase (GAPDH) probe was used as a control.
(B) Immunoblot analysis of m-Numb in adult mouse; 50 μg of protein was used in each lane. α-MNB is the anti-MNBR1 antiserum. PI is a preimmune serum.
(C) T2 RNase protection assay of m-numb expression during mouse embryogenesis; 20 μg of total cytoplasmic RNA from whole embryos was used from each stage. Yeast tRNA was used as a control.
(D) m-Numb expression in the roof of E12.5 mouse telencephalic vesicle. m-Numb was detected by the anti-MNBR1 antibody (in green). V, telencephalic vesicle (ventricular cavity); VZ, ventricular zone; CP, cortical plate.
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4. Figure 3
Asymmetric Localization of Mouse Numb in Mitotic Neural Progenitors of Embryonic Mouse Forebrain
m-Numb staining was in green and propidium iodide chromosome staining (used as an index for the cell cycle status) was in red.
(A) (a) E12.5. Asymmetric localization of m-Numb at apical or apical–lateral cortex of ventricular cells (arrows, also in [b]). (b) E15.5. Membrane association of m-Numb in epithelial cells of the choroid plexus (bracket). (c–g) E12.5. m-Numb staining in prophase (c), metaphase (d), and telophase (e–g) cells of the ventricular zone. (e), (f), and (g) represent three cells with vertical, intermediate, and horizontal division planes, respectively. The ventricular surface is down. The m-Numb staining observed near the basal part of the cells in (e) and (f) originated from neighboring cells, as revealed by confocal scan (data not shown). We cosistently observed stronger m-Numb staining at nascent membranes in telophase cells (e and f). However, only one nascent membrane showed strong m-Numb staining in (f), as revealed by confocal scan (data not shown).
(B) Asymmetric m-Numb localization in a cell of the subventricular zone (arrow).
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5. Figure 4
Asymmetric Localization of Mouse Numb Is Independent of the Orientation of Cleavage Planes
Ventricular cells are from E15.5 mouse forebrain sections. The apical surface is at the bottom. Red, propidium iodide staining of chromosomes. Green, Numb immunoreactivity.
(A) (a–c) An anaphase cell where, based on the chromosome orientation, the cleavage plane (arrowheads) is perpendicular to the ventricular surface and bisects the m-Numb crescent ([c], superimposed images of [a] and [b]). (d–f) An anaphase cell where the cleavage plane is approximately parallel to the ventricular surface and does not intersect the m-Numb crescent ([f], superimposed images of [d] and [e]). The m-Numb staining observed near the basal part of the cell in (a) and (c) originated from a neighboring cell.
(B) A model for symmetric and asymmetric divisions of ventricular cells with respect to the mitotic spindle (in red), the division plane (in brown), and m-Numb segregation (in green). (a) A vertical cell division, with the cleavage plane perpendicular to the ventricular surface (black line) and the m-Numb crescent, generates two daughter cells that remain as progenitors (S, stem cell). (b) A horizontal division, with the cleavage plane parallel to the ventricular surface and the m-Numb crescent, generates one progenitor cell and one neuron (N) that migrates to the cortical plate (arrow). (c) An intermediate cell division, with the cleavage plane at 45° to the ventricular surface and parallel to the apical–lateral m-Numb crescent, also generates one progenitor and one neuron. (d) A hypothetical intermediate cell division, with the cleavage plane at 45° to the ventricular surface but intersecting the m-Numb crescent, generates either two progenitors (Sa and Sb), differing with respect to the amount of m-Numb and perhaps the ultimate cell fates, or one progenitor (Sa) and one neuron (Na). A vertical cleavage plane in combination with an apical–lateral m-Numb crescent could lead to a similar scenario.
(C) A hypothetical dividing ventricular cell with m-Numb and Notch1 (in blue) localized at opposite poles. Separate controls over the mitotic spindle orientaion and the asymmetric localization of m-Numb and Notch1 could generate the different segregation patterns of m-Numb, described in (B), and of Notch1 (Chenn and McConnell 1995).
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6. Figure 5 Asymmetric Localization of Mouse Numb in Drosophila Embryos
(A) Asymmetric localization of m-Numb (in green) in a dividing CNS neuroblast (a) or PNS SOP cell (b). After SOP division, m-Numb is primarily segregated to one daughter cell (c, B cell). Red is Asense (ASE) staining used to identify neuroblasts or SOP cells (Brand et al. 1993).
(B) m-Numb (a, in green, using mouse anti-MYC) and d-Numb (b, in red, using rabbit anti-d-Numb) are localized to the same side in a dividing neuroblast (c, superimposed).
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7. Figure 6 Rescue of the Drosophila numb Mutant Phenotype by Mouse Numb
(A) Neuronal rescue. PNS neurons visualized by MAb22C10 (in green) in embryos from wild-type (a)numb mutant (b), and numb mutant expressing either m-Numb (c) or d-Numb (d). Embryos are arranged with anterior to the left and dorsal on top.
(B) Sheath cell rescue. Two dorsal-most es organs (a, schematic) in abdominal hemisegments of embryos from wild-type (b–d)numb mutant (e–g), and numb mutant expressing m-Numb (h–j). Green is Prospero staining identifying sheath cells (b, e, and h, arrows), while red is Cut staining identifying all eight cells of the two es organs (c, f and i, bracketed). (d), (g), and (j) are respective superimposed images.
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8. Figure 7 Physical Interaction of m-Numb and Notch1
GST–NICD, fusion protein of GST and Notch1 intracellular domain.
(A) Copurification of m-Numb and Notch1 ICD. Immunoblot analysis of m-Numb in proteins purified by glutathione–agarose beads. Lane 1, GST–NICD alone; lanes 2–7, no fusion protein (minus), GST, and GST–NICD, respectively, in the presence of crude liver extracts from mouse (lanes 2–4) or in vitro translated m-Numb (lanes 5–7). In vitro translated m-Numb contains a MYC epitope tag at the N-terminus (MYC–m-Numb, see Experimental Procedures; lane 7), and therefore appears to be larger than the major endogenous m-Numb band (lane 4). The amount of GST used (lanes 3 and 6) is ∼10 times that of GST–NICD (lanes 4 and 7).
(B) m-Numb binds to specific regions of Notch1 ICD. Immunoblot analysis of in vitro translated m-Numb in proteins purified by glutathione–agarose beads using various regions of Notch1 ICD. F, full-length GST–NICD; N, fusion protein of GST and N-terminal (pre-CDC10/ankyrin repeats) portion of Notch1 ICD; A, fusion protein of GST and CDC10/ankyrin repeats; C, fusion protein of GST and C-terminal (post-CDC10/ankyrin repeats) portion of Notch1 ICD.
(C) The conserved domain of m-Numb binds to Notch1 ICD. Autoradiography of 35S-Met labeled, in vitro translated m-Numb (PvuII-truncated, amino acids 1–282) copurified by glutathione–agarose beads in the presence of either GST (lane 1) or GST–NICD (lane 2).
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